FDA Device Intelligence
Home › Novasignal Corp. › Temporal Monitoring Headframe Foam Procedural Set, Packaged 10-Pack

Temporal Monitoring Headframe Foam Procedural Set, Packaged 10-Pack

Novasignal Corp. · Model NA-DSP3PK · UDI-DI 10850681007174

ITXIYN Prescription
1
510(k) clearances
4,015
Adverse events (23 deaths)
147
Recalls
396
Facilities

Description

A box of 10 procedural sets that include replacement foam for the Temporal Monitoring Headframe.

Recalls

DateFirmReason
2025-11-17Sheathing Technologies IncVaginal/rectal ultrasound probe covers with a viral barrier may have product defects, which may result in contamination during use, posing an infection risk.
2025-09-05Philips Ultrasound, IncTo provide clarification and labelling to define the useful life of ultrasound transducers in the field.
2025-09-05Philips Ultrasound, IncTo provide clarification and labelling to define the useful life of ultrasound transducers in the field.
2025-09-05Philips Ultrasound, IncTo provide clarification and labelling to define the useful life of ultrasound transducers in the field.
2025-09-05Philips Ultrasound, IncTo provide clarification and labelling to define the useful life of ultrasound transducers in the field.
2025-09-05Philips Ultrasound, IncTo provide clarification and labelling to define the useful life of ultrasound transducers in the field.
2025-09-05Philips Ultrasound, IncTo provide clarification and labelling to define the useful life of ultrasound transducers in the field.
2025-09-05Philips Ultrasound, IncTo provide clarification and labelling to define the useful life of ultrasound transducers in the field.
2025-09-05Philips Ultrasound, IncTo provide clarification and labelling to define the useful life of ultrasound transducers in the field.
2025-09-05Philips Ultrasound, IncTo provide clarification and labelling to define the useful life of ultrasound transducers in the field.

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.